The DOI matches its Crossref record; 78 of the 78 references it cites were found in a registry or an index.
Stem cells in postnatal myogenesis: molecular mechanisms of satellite cell quiescence, activation and replenishment
Abstract
Satellite cells are the primary stem cells in adult skeletal muscle, and are responsible for postnatal muscle growth, hypertrophy and regeneration. In mature muscle, most satellite cells are in a quiescent state, but they activate and begin proliferating in response to extrinsic signals. Following activation, a subset of satellite cell progeny returns to the quiescent state during the process of self-renewal. Here, we review recent studies of satellite cell biology and focus on the key transitions from the quiescent state to the state of proliferative activation and myogenic lineage progression and back to the quiescent state. The molecular mechanisms of these transitions are considered in the context of the biology of the satellite cell niche, changes with age, and interactions with established pathways of myogenic commitment and differentiation.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“This rapid repair process is carried out mainly by satellite cells with a contribution of NO. 41”
From Dietary nitrate supplementation improves revascularization in chronic ischemia (2012) · cites this paper as [41]
Citations
Cites
SATELLITE CELL OF SKELETAL MUSCLE FIBERS
Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683
Muscle Regeneration by Bone Marrow-Derived Myogenic Progenitors
Ferrari, G., Cusella, G., Angelis, D., Coletta, M., Paolucci, E., Stornaiuolo, A., Cossu, G., & Mavilio, F. (1998) · Science · doi:10.1126/science.279.5356.1528 · Cited by 2,721
Cellular and Molecular Regulation of Muscle Regeneration
CHARGÉ, S. B. P., & Rudnicki, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00019.2003 · Cited by 2,691
Pax7 Is Required for the Specification of Myogenic Satellite Cells
Seale, P., Sabourin, L. A., Girgis-Gabardo, A., Mansouri, A., Gruß, P., & Rudnicki, M. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00066-0 · Cited by 2,345
Rejuvenation of aged progenitor cells by exposure to a young systemic environment
Conboy, I. M., Conboy, M. J., Wagers, A. J., Girma, E. R., Weissman, I. L., & Rando, T. A. (2005) · Nature · doi:10.1038/nature03260 · Cited by 2,287
Self-citationWeissman, I. L. (2000) · Cell · doi:10.1016/s0092-8674(00)81692-x · Cited by 1,827
Myogenic satellite cells: physiology to molecular biology
Hawke, T. J., & Garry, D. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.2.534 · Cited by 1,646
Little Evidence for Developmental Plasticity of Adult Hematopoietic Stem Cells
Wagers, A. J., Sherwood, R. I., Christensen, J. L., & Weissman, I. L. (2002) · Science · doi:10.1126/science.1074807 · Cited by 1,460
Collins, C. A., Olsen, I., Zammit, P. S., Heslop, L., Petrie, A., Partridge, T. A., & Morgan, J. E. (2005) · Cell · doi:10.1016/j.cell.2005.05.010 · Cited by 1,445
The E2F transcription factor is a cellular target for the RB protein
Chellappan, S., Hiebert, S. W., Mudryj, M. M., Horowitz, J. M., & Nevins, J. R. (1991) · Cell · doi:10.1016/0092-8674(91)90557-f · Cited by 1,415
Cited by
Sorted by citations
Stem Cells and Niches: Mechanisms That Promote Stem Cell Maintenance throughout Life
Morrison, S. J., & Spradling, A. C. (2008) · Cell · doi:10.1016/j.cell.2008.01.038 · Cited by 2,026
Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis
Joe, A. W. B., Yi, L., Natarajan, A., Le Grand, F., So, L., Wang, J., Rudnicki, M. A., & Rossi, F. M. V. (2010) · Nature Cell Biology · doi:10.1038/ncb2015 · Cited by 1,690
Geriatric muscle stem cells switch reversible quiescence into senescence
Sousa-Victor, P., Gutarra, S., García-Prat, L., Rodriguez-Ubreva, J., Ortet, L., Ruiz-Bonilla, V., Jardí, M., Ballestar, E., González, S., Serrano, A. L., et al. (2014) · Nature · doi:10.1038/nature13013 · Cited by 1,010
Pax7-expressing satellite cells are indispensable for adult skeletal muscle regeneration
Sambasivan, R., Yao, R., Kissenpfennig, A., Van Wittenberghe, L., Paldi, A., Gayraud-Morel, B., Guenou, H., Malissen, B., Tajbakhsh, S., & Galy, A. (2011) · Development · doi:10.1242/dev.067587 · Cited by 939
Reversal of Cancer Cachexia and Muscle Wasting by ActRIIB Antagonism Leads to Prolonged Survival
Zhou, X., Wang, J. L., Lu, J., Song, Y., Kwak, K. S., Jiao, Q., Rosenfeld, R., Chen, Q., Boone, T. C., Simonet, W. S., et al. (2010) · Cell · doi:10.1016/j.cell.2010.07.011 · Cited by 960
Interleukin-6 Is an Essential Regulator of Satellite Cell-Mediated Skeletal Muscle Hypertrophy
Serrano, A. L., Baeza-Raja, B., Perdiguero, E., Jardí, M., & Muñoz-Cánoves, P. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.11.011 · Cited by 873
Muscle Satellite Cells and Endothelial Cells: Close Neighbors and Privileged Partners
Christov, C., Chrétien, F. C., Abou-Khalil, R., Bassez, G., Vallet, G., Authier, F., Bassaglia, Y., Shinin, V., Tajbakhsh, S., Chazaud, B., et al. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-08-0693 · Cited by 702
Repairing skeletal muscle: regenerative potential of skeletal muscle stem cells.
Tedesco, F. S., Dellavalle, A., Díaz-Manera, J., Messina, G., & Cossu, G. (2010) · Journal of Clinical Investigation · doi:10.1172/jci40373 · Cited by 667
Pax7 and myogenic progression in skeletal muscle satellite cells
Zammit, P. S., Relaix, F., Nagata, Y., Ruiz, A. P., Collins, C. A., Partridge, T. A., & Beauchamp, J. R. (2006) · Journal of Cell Science · doi:10.1242/jcs.02908 · Cited by 614
Notch Signaling Is Necessary to Maintain Quiescence in Adult Muscle Stem Cells
Bjornson, C. R. R., Cheung, T. H., Liu, L., Tripathi, P. V., Steeper, K. M., & Rando, T. A. (2012) · Stem Cells · doi:10.1002/stem.773 · Cited by 598
Self-citationPedersen, B. K. (2013) · Comprehensive physiology · doi:10.1002/cphy.c120033 · Cited by 516
Satellite-cell pool size does matter: Defining the myogenic potency of aging skeletal muscle
Shefer, G., de Mark, D. P. V., Richardson, J. B., & Yablonka‐Reuveni, Z. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.02.022 · Cited by 526
Muscle stem cells in development, regeneration, and diseasePreprint
Shi, X., & Garry, D. J. (2006) · Genes & Development · doi:10.1101/gad.1419406 · Cited by 502
Satellite cell content is specifically reduced in type II skeletal muscle fibers in the elderly
Verdijk, L. B., Koopman, R., Schaart, G., Meijer, K., Savelberg, H. H. C. M., & van Loon, L. J. C. (2007) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00278.2006 · Cited by 489
Highly Efficient, Functional Engraftment of Skeletal Muscle Stem Cells in Dystrophic Muscles
Cerletti, M., Jurga, S., Witczak, C. A., Hirshman, M. F., Shadrach, J. L., Goodyear, L. J., & Wagers, A. J. (2008) · Cell · doi:10.1016/j.cell.2008.05.049 · Cited by 472
Myogenic progenitor cells and skeletal myogenesis in vertebrates
BUCKINGHAM, M. E. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.08.008 · Cited by 452
Mimeault, M., Hauke, R. J., & Batra, S. K. (2007) · Clinical Pharmacology & Therapeutics · doi:10.1038/sj.clpt.6100301 · Cited by 451
New fundamental resistance exercise determinants of molecular and cellular muscle adaptations
Toigo, M., & Boutellier, U. (2006) · European Journal of Applied Physiology · doi:10.1007/s00421-006-0238-1 · Cited by 437
Petrella, J. K., Kim, J.-S., Mayhew, D. L., Cross, J. M., & Bamman, M. M. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01215.2007 · Cited by 435
miR-206 and -486 Induce Myoblast Differentiation by Downregulating Pax7
Dey, B. K., Gagan, J. R., & Dutta, A. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01009-10 · Cited by 380
Fat cells reactivate quiescent neuroblasts via TOR and glial insulin relays in Drosophila
Sousa‐Nunes, R., Yee, L. L., & Gould, A. P. (2011) · Nature · doi:10.1038/nature09867 · Cited by 406
Satellite cells in human skeletal muscle; from birth to old age
Verdijk, L. B., Snijders, T., Drost, M., Delhaas, T., Kadi, F., & van Loon, L. J. C. (2014) · AGE · doi:10.1007/s11357-013-9583-2 · Cited by 399
Palacios, D., Mozzetta, C., Consalvi, S., Caretti, G., Saccone, V., Proserpio, V., Marquez, V. E., Valente, S., Mai, A., Forcales, S. V., et al. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.08.013 · Cited by 392
Verdijk, L. B., Gleeson, B. G., Jonkers, R. A. M., Meijer, K., Savelberg, H. H. C. M., Dendale, P., & van Loon, L. J. C. (2009) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/gln050 · Cited by 372
Skeletal muscle stem cells in developmental versus regenerative myogenesis
Tajbakhsh, S. (2009) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2009.02158.x · Cited by 333
Effects of RAS on the genesis of embryonal rhabdomyosarcoma
Langenau, D. M., Keefe, M. D., Storer, N. Y., Guyon, J. R., Kutok, J. L., Le, X., Goessling, W., Neuberg, D. S., Kunkel, L. M., & Zon, L. I. (2007) · Genes & Development · doi:10.1101/gad.1545007 · Cited by 320
Regulatory factors and cell populations involved in skeletal muscle regeneration
Broek, R. W. T., Grefte, S., & den Hoff, J. W. V. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22127 · Cited by 315
Myostatin/activin pathway antagonism: molecular basis and therapeutic potential
Han, H. Q., Zhou, X., Mitch, W. E., & Goldberg, A. L. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.05.019 · Cited by 314
Maintaining Tissue Homeostasis: Dynamic Control of Somatic Stem Cell Activity
Biteau, B., Hochmuth, C. E., & Jasper, H. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.10.004 · Cited by 322
Windhorst, R. A., Cohen, S. H., Hathi, N. P., McCarthy, P. J., Ryan, R. E., Yan, H., Baldry, I. K., Driver, S. P., Frogel, J. A., Hill, D. T., et al. (2011) · The Astrophysical Journal Supplement Series · doi:10.1088/0067-0049/193/2/27 · Cited by 298
Muscle injuries and strategies for improving their repair
Laumonier, T., & Ménétrey, J. (2016) · Journal of Experimental Orthopaedics · doi:10.1186/s40634-016-0051-7 · Cited by 297
Myogenic regulatory factors: The orchestrators of myogenesis after 30 years of discovery
Asfour, H. A., Allouh, M. Z., & Said, R. S. (2018) · Experimental Biology and Medicine · doi:10.1177/1535370217749494 · Cited by 257
Juhas, M., Engelmayr, G. C., Fontanella, A. N., Palmer, G. M., & Bursac, N. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402723111 · Cited by 246
Regulation of muscle growth in neonates
Davis, T. A., & Fiorotto, M. L. (2008) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e32831cef9f · Cited by 244
Does Exercise-Induced Muscle Damage Play a Role in Skeletal Muscle Hypertrophy?
Schoenfeld, B. J. (2012) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0b013e31824f207e · Cited by 258
Macrophages provide a transient muscle stem cell niche via NAMPT secretion
Ratnayake, D., Nguyen, P. D., Rossello, F. J., Wimmer, V. C., Tan, J. L., Galvis, L. A., Julier, Z., Wood, A. J., Boudier, T., Isiaku, A. I., et al. (2021) · Nature · doi:10.1038/s41586-021-03199-7 · Cited by 239
miR-26a is required for skeletal muscle differentiation and regeneration in micePreprint
Dey, B. K., Gagan, J., Yan, Z., & Dutta, A. (2012) · Genes & Development · doi:10.1101/gad.198085.112 · Cited by 218
Inflammaging: Implications in Sarcopenia
Antuña, E., Cachán-Vega, C., Bermejo-Millo, J. C., Potes, Y., Caballero, B., Vega‐Naredo, I., Coto‐Montes, A. M., & García-González, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315039 · Cited by 234
Sun, L., Ma, K., Wang, H., Xiao, F., Gao, Y., Zhang, W., Wang, K., Gao, X., Ip, N. Y., & Wu, Z. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200703184 · Cited by 214
Skeletal Muscle Development and Regeneration
Grefte, S., Kuijpers‐Jagtman, A. M., Torensma, R., & den Hoff, J. W. V. (2007) · Stem Cells and Development · doi:10.1089/scd.2007.0058 · Cited by 197
Cell death, clearance and immunity in the skeletal muscle
Sciorati, C., Rigamonti, E., Manfredi, A. A., & Rovere, P. Q. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2015.171 · Cited by 205
Dacwag, C. S., Ohkawa, Y., Pal, S., Sif, S., & Imbalzano, A. N. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.01528-06 · Cited by 191
Recent Progress on Tissue-Resident Adult Stem Cell Biology and Their Therapeutic Implications
Mimeault, M., & Batra, S. K. (2008) · Stem Cell Reviews and Reports · doi:10.1007/s12015-008-9008-2 · Cited by 194
Rossi, C. A., Flaibani, M., Blaauw, B., Pozzobon, M., Figallo, E., Reggiani, C., Vitiello, L., Elvassore, N., & Coppi, P. D. (2011) · The FASEB Journal · doi:10.1096/fj.10-174755 · Cited by 184
Kornasio, R., Riederer, I., Butler-Browne, G. S., Mouly, V., Uni, Z., & Halevy, O. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2008.12.017 · Cited by 184
Maternal obesity downregulates myogenesis and β-catenin signaling in fetal skeletal muscle
Tong, J. F., Yan, X., Zhu, M. J., Ford, S. P., Nathanielsz, P. W., & Du, . (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.90924.2008 · Cited by 181
A Murine Model of Volumetric Muscle Loss and a Regenerative Medicine Approach for Tissue Replacement
Sicari, B. M., Agrawal, V., Siu, B. F., Medberry, C. J., Dearth, C. L., Turner, N. J., & Badylak, S. F. (2012) · Tissue Engineering Part A · doi:10.1089/ten.tea.2012.0475 · Cited by 176
Extracellular Matrix Regulation of Stem Cell Behavior
Ahmed, M., & ffrench‐Constant, C. (2016) · Current Stem Cell Reports · doi:10.1007/s40778-016-0056-2 · Cited by 182
Heterogeneity in the muscle satellite cell population
Biressi, S., & Rando, T. A. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.09.003 · Cited by 168
Self-citationModifying muscle mass – the endocrine perspective
Solomon, A. M., & Bouloux, P. M. G. (2006) · Journal of Endocrinology · doi:10.1677/joe.1.06837 · Cited by 156
Concise Review: Stem Cells, Myocardial Regeneration, and Methodological Artifacts
Anversa, P., Leri, A., Rota, M., Hosoda, T., Bearzi, C., Urbanek, K., Kajstura, J., & Bolli, R. (2006) · Stem Cells · doi:10.1634/stemcells.2006-0623 · Cited by 158
JAK2/STAT2/STAT3 Are Required for Myogenic Differentiation
Wang, K., Wang, C., Xiao, F., Wang, H., & Wu, Z. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m803012200 · Cited by 150
Refining the role for adult stem cells as cancer cells of origin
White, A. C., & Lowry, W. E. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.08.008 · Cited by 157
LIF is a contraction-induced myokine stimulating human myocyte proliferation
Broholm, C., Laye, M. J., Brandt, C., Vadalasetty, R., Pilegaard, H., Pedersen, B. K., & Scheele, C. C. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01399.2010 · Cited by 155
A Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice
Biressi, S., Miyabara, E. H., Gopinath, S. D., Carlig, P. M. M., & Rando, T. A. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008411 · Cited by 152
Self-citationAre Human and Mouse Satellite Cells Really the Same?
Boldrin, L., Muntoni, F., & Morgan, J. E. (2010) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2010.956201 · Cited by 155
Biomaterial-based delivery for skeletal muscle repair
Cezar, C. A., & Mooney, D. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.09.008 · Cited by 127
Cosgrove, B. D., Sacco, A., Gilbert, P. M., & Blau, H. M. (2009) · Differentiation · doi:10.1016/j.diff.2009.08.004 · Cited by 141
Boonen, K. J. M., Rosaria-Chak, K. Y., Baaijens, F. F., van der Schaft, D. W. J., & Post, M. J. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00015.2009 · Cited by 135
Adult stem cells and their trans-differentiation potential—perspectives and therapeutic applications
Hombach‐Klonisch, S., Panigrahi, S., Rashedi, I., Seifert, A., Alberti, E., Pocar, P., Kurpisz, M. K., Schulze‐Osthoff, K., Mackiewicz, A. A., & Łoś, M. (2008) · Journal of Molecular Medicine · doi:10.1007/s00109-008-0383-6 · Cited by 140
Zhang, J., Xiao, Z., Qu, C., Cui, W., Wang, X., & Du, J. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1303486 · Cited by 139
Dentice, M., Ambrosio, R., Damiano, V., Sibilio, A., Luongo, C., Guardiola, O., Yennek, S., Zordan, P., Minchiotti, G., Colao, A., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.10.009 · Cited by 131
Sebastian, S., Sreenivas, P., Sambasivan, R., Cheedipudi, S. M., Kandalla, P. K., Pavlath, G. K., & Dhawan, J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807136106 · Cited by 127
Self-citationLong noncoding RNA Neat1 modulates myogenesis by recruiting Ezh2
Wang, S., Zuo, H., Jin, J., Lv, W., Xu, Z., Fan, Y., Zhang, J., & Zuo, B. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1742-7 · Cited by 126
Stem cells in the hood: the skeletal muscle niche
Pannérec, A., Marazzi, G., & Sassoon, D. A. (2012) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2012.07.004 · Cited by 130
Satellite Cells Contribution to Exercise Mediated Muscle Hypertrophy and Repair.
Bazgir, B., Fathi, R., Valojerdi, M. R., Mozdziak, P. E., & Asgari, A. (2017) · PubMed Central · doi:10.22074/cellj.2016.4714 · Cited by 124
Modeling human muscle disease in zebrafish
Guyon, J. R., Steffen, L. S., Howell, M. H., Pusack, T. J., Lawrence, C., & Kunkel, L. M. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2006.07.003 · Cited by 130
Bower, N. I., & Johnston, I. A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011100 · Cited by 120
Takubo, K., Ohmura, M., Azuma, M., Nagamatsu, G., Yamada, W., Arai, F., Hirao, A., & Suda, T. (2008) · Cell stem cell · doi:10.1016/j.stem.2007.10.023 · Cited by 122
The Hippo Pathway Regulates Neuroblasts and Brain Size in Drosophila melanogaster
Poon, C. L. C., Mitchell, K. A., Kondo, S., Cheng, L. Y., & Harvey, K. F. (2016) · Current Biology · doi:10.1016/j.cub.2016.02.009 · Cited by 113
The Muscle Stem Cell Niche: Regulation of Satellite Cells During Regeneration
Boonen, K. J. M., & Post, M. J. (2008) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2008.0045 · Cited by 114
Dietary nitrate supplementation improves revascularization in chronic ischemia
Hendgen-Cotta, U. B., Luedike, P., Totzeck, M., Kropp, M., Schicho, A., Stock, P., Rammos, C., Niessen, M., Heiss, C., Lundberg, J. O., et al. (2012) · Circulation · doi:10.1161/circulationaha.112.112912 · Cited by 110
Yamada, M., Tatsumi, R., Yamanouchi, K., Hosoyama, T., SHIRATSUCHI, S., Satô, A., Mizunoya, W., Ikeuchi, Y., Furuse, M., & Allen, R. E. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00449.2009 · Cited by 113
Noncoding RNAs, Emerging Regulators of Skeletal Muscle Development and Diseases
Nie, M., Deng, Z., Liu, J., & Wang, D. (2015) · BioMed Research International · doi:10.1155/2015/676575 · Cited by 105
Genome amplification and cellular senescence are hallmarks of human placenta development
Velicky, P., Meinhardt, G., Plessl, K., Vondra, S., Weiss, T., Haslinger, P., Lendl, T., Aumayr, K., Mairhofer, M., Zhu, X., et al. (2018) · PLOS Genetics · doi:10.1371/journal.pgen.1007698 · Cited by 102
High glucose inhibits myogenesis and induces insulin resistance by down-regulating AKT signaling
Luo, W., Ai, L., Wang, B., & Zhou, Y. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109498 · Cited by 101
The IGF‐I splice variant MGF increases progenitor cells in ALS, dystrophic, and normal muscle
Ateş, K., Yang, S. Y., Orrell, R. W., Sinanan, A., Simons, J. P., Solomon, A., Beech, S., Goldspink, G., & Lewis, M. P. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.05.030 · Cited by 99
Huang, C., Li, Y. H., Hu, S., Chi, J. R., Lin, G., Lin, C. C., Gong, H., Chen, J., Chen, R. H., Chang, S., et al. (2012) · Journal of Animal Science · doi:10.2527/jas.2012-5142 · Cited by 101
PPARs and Microbiota in Skeletal Muscle Health and Wasting
Manickam, R., Duszka, K., & Wahli, W. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218056 · Cited by 104
Drummond, M. J., Miyazaki, M., Dreyer, H. C., Pennings, B., Dhanani, S., Volpi, E., Esser, K. A., & Rasmussen, B. B. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.90842.2008 · Cited by 100
Isolation, Characterization, Differentiation, and Application of Adipose-Derived Stem Cells
Kuhbier, J. W., Weyand, B., Radtke, C., Vogt, P. M., Kasper, C., & Reimers, K. (2010) · Springer eBooks · doi:10.1007/10_2009_24 · Cited by 99
Isolation and characterization of porcine adult muscle‐derived progenitor cells
Wilschut, K. J., Jaksani, S., van den Dolder, J., Haagsman, H. P., & Roelen, B. A. J. (2008) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21921 · Cited by 97
Zhang, D., Li, X., Chen, C., Li, Y., Zhao, L., Jing, Y., Liu, W., Wang, X., Zhang, Y., Xia, H., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041478 · Cited by 96
Eccentric Exercise Increases Satellite Cell Content in Type II Muscle Fibers
Cermak, N. M., Snijders, T., McKay, B. R., Parise, G., Verdijk, L. B., Tarnopolsky, M. A., Gibala, M. J., & van Loon, L. J. C. (2013) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e318272cf47 · Cited by 95
Dogra, C., Hall, S. L., Wedhas, N., Linkhart, T. A., & Kumar, A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m608668200 · Cited by 91
Dayanidhi, S., & Lieber, R. L. (2014) · Muscle & Nerve · doi:10.1002/mus.24441 · Cited by 99
LIF-Dependent Signaling: New Pieces in the Lego
Mathieu, M.-E., Saucourt, C., Mournetas, V., Gauthereau, X., Thézé, N., Praloran, V., Thiébaud, P., & Bœuf, H. (2011) · Stem Cell Reviews and Reports · doi:10.1007/s12015-011-9261-7 · Cited by 96
Myf5 haploinsufficiency reveals distinct cell fate potentials for adult skeletal muscle stem cells
Gayraud-Morel, B., Chrétien, F. C., Jory, A., Sambasivan, R., Négroni, E., Flamant, P., Soubigou, G., Coppée, J., Santo, J. P. D., Cumano, A., et al. (2012) · Journal of Cell Science · doi:10.1242/jcs.097006 · Cited by 92
Skeletal Muscle as a Paradigm for Regenerative Biology and Medicine
Gayraud-Morel, B., Chrétien, F., & Tajbakhsh, S. (2009) · Regenerative Medicine · doi:10.2217/17460751.4.2.293 · Cited by 103
Fibronectin promotes migration, alignment and fusion in an in vitro myoblast cell model
Vaz, R., Martins, G. G., Þorsteinsdóttir, S., & Rodrigues, G. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1364-1 · Cited by 92
Blood Vessels and the Satellite Cell Niche
Mounier, R., Chrétien, F., & Chazaud, B. (2011) · Current Topics in Developmental Biology · doi:10.1016/b978-0-12-385940-2.00005-x · Cited by 89
Stem Cells for Skeletal Muscle Tissue Engineering
Pantelic, M. N., & Larkin, L. M. (2018) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2017.0451 · Cited by 88
Generation of transplantable, functional satellite‐like cells from mouse embryonic stem cells
Chang, H. C., Yoshimoto, M., Umeda, K., Iwasa, T., Mizuno, Y., Fukada, S., Yamamoto, H., Motohashi, N., Miyagoe‐Suzuki, Y., Takeda, S., et al. (2009) · The FASEB Journal · doi:10.1096/fj.08-123661 · Cited by 88
Senesi, P., Luzi, L., Montesano, A., Mazzocchi, N., & Terruzzi, I. (2013) · Journal of Translational Medicine · doi:10.1186/1479-5876-11-174 · Cited by 90
Collins, C. A. (2006) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2006.01.006 · Cited by 87
Sphingosine 1-phosphate stimulates proliferation and migration of satellite cells
Calise, S. J., Blescia, S., Cencetti, F., Bernacchioni, C., Donati, C., & Bruni, P. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.11.016 · Cited by 86
Imprinted Genes That Regulate Early Mammalian Growth Are Coexpressed in Somatic Stem Cells
Berg, J. S., Lin, K. K., Sonnet, C., Boles, N. C., Weksberg, D. C., Nguyen, H., Holt, L. J., Rickwood, D., Daly, R. J., & Goodell, M. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026410 · Cited by 84
Ohkawa, Y., Yoshimura, S., Higashi, C., Marfella, C. G. A., Dacwag, C. S., Tachibana, T., & Imbalzano, A. N. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m608898200 · Cited by 85
McKay, B. R., Toth, K., Tarnopolsky, M. A., & Parise, G. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.190876 · Cited by 83
Growth Factors for Skeletal Muscle Tissue Engineering
Syverud, B. C., VanDusen, K. W., & Larkin, L. M. (2016) · Cells Tissues Organs · doi:10.1159/000444671 · Cited by 82
Metadata
- Authors
- Dhawan, J., & Rando, T. A.
- Affiliations
- Centre for Cellular and Molecular Biology (IN)
- VA Palo Alto Health Care System (US)
- Corresponding author
- Rando, Thomas A.
- Venue
- Trends in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2005-12
- Volume
- 15
- Issue
- 12
- Pages
- 666-673
- ISSN
- 0962-8924 (ISSN-L)
- OpenAlex
- W2054692433
- Cited by
- 466
- References
- 78
- Citations by year
- 2026: 7 · 2025: 10 · 2024: 6 · 2023: 18 · 2022: 16 · 2021: 22 · 2020: 18 · 2019: 18 · 2018: 11 · 2017: 26 · 2016: 18 · 2015: 25 · 2014: 27 · 2013: 34 · 2012: 40
- FWCI
- 2.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- satellite cells, skeletal muscle stem cells, quiescence, cell activation, self-renewal, muscle regeneration, muscle hypertrophy, aging, myogenesis
- MeSH terms
- Animals, Cell Cycle, Cell Differentiation, Humans, Stem Cells, Gene Expression Regulation, Developmental, Muscle Development, Satellite Cells, Skeletal Muscle, Cell Proliferation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review